Jobs at Cellares

The Manufacturing Supervisor oversees cGMP operations and manages the production of cell therapy products, ensuring compliance, team development, and process optimization.

Lead system requirements, architecture, modeling, and verification for a cell therapy manufacturing platform. Support subsystem teams, perform system characterization, root-cause analysis, and drive design convergence and continuous improvement from R&D toward scale-up.

The Senior Director, Supply Chain leads and develops the Supply Chain organization, implementing strategies for efficiency in materials management, logistics, and production planning within a biotech environment.

Support MSAT technology transfer and scale-up for cell therapy manufacturing. Drive process automation, ensure GMP readiness, maintain process knowledge and capability through data analysis, lead root cause investigations, CAPA, change control, FMEA, and validation activities. Write SOPs and batch records, define equipment requirements, provide training, and coordinate cross-functional stakeholders.

Support design and execution of small-scale and scale-up cell therapy process development experiments using the Cellares platform. Perform cell line maintenance, leukopak processing, gene modification, expansion, cryopreservation, equipment qualification, SOP/report authoring, data analysis, and routine lab tasks to advance automated cell therapy manufacturing processes.

Design and execute cell therapy process development and scale-up experiments, maintain primary cell lines and leukopaks, draft SOPs and batch documentation, analyze process data, troubleshoot semi-automated instruments and LIMS, and implement corrective actions to advance the Cellares automated cell therapy manufacturing platform.

The Senior Electrical Engineer will lead electrical design for automation equipment, ensuring compliance and managing design documentation. Responsibilities include collaborating with teams, conduct prototyping, and driving design reviews based on industry standards.

The Director of Enterprise Programs leads client programs in process development, managing teams, overseeing tech transfer, ensuring compliance, and optimizing manufacturing processes for cell therapies.

The Quality Control Analyst will perform analytical testing, including in-process, lot release, and stability testing while ensuring compliance with cGMP guidelines. They will also investigate discrepancies and support equipment validation and documentation for regulatory submissions.

The HR Business Partner serves as the on-site HR resource, providing employee support and managing HR processes in a manufacturing environment while partnering with leadership to ensure compliance and improve HR practices.

Cellares seeks a Senior Scientist in Process Development to execute and analyze experiments for cell therapy, interface cross-functionally, and mentor junior staff.

Lead and execute stabilization, scaling, and continuous improvement of GMP-critical systems (ERP, MES, QMS, PLM, LIMS, integrations). Act as a hands-on player-coach bridging Manufacturing, Quality, Supply Chain, Engineering, and Finance to ensure data integrity, traceability, audit readiness, and operational execution while governing releases, validations, vendor performance, and cross-system issue resolution.

The Manufacturing Support Services Specialist supports manufacturing and warehouse operations, performing routine procedures in a GMP environment, training new associates, and ensuring compliance with SOPs and safety policies.

Lead MSAT process knowledge, technology transfers, and process automation for cell therapy manufacturing. Drive GMP readiness, process validation, CAPA/FMEA, documentation, root-cause investigations, capacity modeling, and cross-functional stakeholder coordination to scale and improve manufacturing operations.

The Automation Engineer will develop and optimize lab automation systems, validate QC workflows, and ensure functionality of automated systems for cell therapy manufacturing.

Lead process development and technology transfer for autologous and allogeneic cell therapies, manage and mentor teams, coordinate cross-functional programs, author technical documentation, and evaluate new technologies to optimize the Cellares manufacturing platform.

This role involves supporting cell therapy manufacturing processes, leading technology transfers, developing automation, ensuring GMP compliance, and collaborating across departments.

The Automation Equipment Engineer will monitor, troubleshoot, and enhance automation equipment, collaborating with teams to resolve issues and improve production systems.

Design and execute experiments (including DOE) to develop and scale cell therapy processes. Collaborate cross-functionally to transfer technologies, author technical documentation, analyze and present results, train staff, troubleshoot processes, and provide technical feedback to engineering and manufacturing teams.

The Director, Operations Finance will oversee FP&A for the Operations organization, driving financial insights, cost forecasts, and operational efficiencies across manufacturing sites globally.